Additional reaction involving diperoxyfumarate and compounds having diperoxysuccinyl groups

ABSTRACT

A DIESTER OF DIPEROXYFUMARIC ACID IS REACTED AT ITS DOBLE BOND WITH AN ORGANIC COMPOUND R-(X)S WHERE X IS A MONOVALENT ATOM READILY ABSTRACTABLE BY A FREE RADICAL, E.G., HYDROGEN, CHLORINE OR BROMINE, AND R IS INERT TO THE PERIOXYCARBONYL GROUPS OF THE DIPEROXYFUMARATE TO FORM AN ADDITION PRODUCT INCLUDING AT LEATS ONE DIESTER OF A SUBSTITUTED DIPEROXYSUCCINIC ACID. FOR EXAMPLE: TETRAHYDROFURAN AND DI-T-BUTYL DIPEROXYFUMARATE REACT AT ABOUT 0* C. TO FORM DI-T-BUTYL ALPHA-(2TETRAHYDROFURYL) DIPEROXYSUCCINATE. POLYGLYCOLS AND POLYVINYL ETHERS, ALCOHOLS, HALIDES, ECT. REACT TO GIVE POLYMERS HAVING PENDANT PAIRS OF PEROXYCARBONYL ESTER GROUPS IN GAMMA RELATIONSHIP TO EACH OTHER. THESE COMPOUNDS ARE OF ESPECIAL INTEREST IN THE PREPARATION OF BLOCK AND GRAFT COPOLYMERS.

United States Patent ADDITIONAL REACTION INVOLVING DIPEROXY- FUMARATE AND COMPOUNDS HAVING DI- PEROXYSUCCINY L GROUPS Richard Anthony Batiord, 456 Forbes Ave., Tonawanda, NY. 14151; Ernest Rudolph Kamens, 52 Rano St., Buflfalo, NY. 14207; and Orville Leonard Mageli, 81 Danbury Lane, Kenmore, N.Y. 14217 No Drawing. Original application Mar. 8, 1968, Ser. No. 711,502, now Patent No. 3,592,948. Divided and this application Apr. 2, 1971, Ser. No. 130,794

Int. Cl. C07c 69/00 US. Cl. 260-453 R 9 Claims ABSTRACT OF THE DISCLOSURE A diester of diperoxyfumaric acid is reacted at its double bond with an organic compound 'R-(X), where X is a monovalent atom readily abstractable by a free radical, e.g., hydrogen, chlorine or bromine, and R is inert to the peroxycarbonyl groups of the diperoxyfumarate to form an addition product including at least one diester of a substituted diperoxysuccinic acid. For example: Tetrahydrofuran and di-t-butyl diperoxyfumarate react at about 0 C. to form di-t-butyl alpha-(2- tetra'hydrofuryl)diperoxysuccinate. Poly-glycols and polyvinyl ethers, alcohols, halides, etc. react to give polymers having pendant pairs of peroxycarbonyl ester groups in gamma relationship to each other.

These compounds are of especial interest in the preparation of block and graft copolymers.

CROSS REFERENCE TO RELATED APPLICATION This application is a division of copending application Ser. No. 711,502, filed Mar. 8, 1968, now US. Pat. 3,592,948.

BACKGROUND OF THE INVENTION (1) Field of the invention This invention relates to diesters of substituted diperoxysuccinic acid, which may be simple molecular compounds or polymeric compounds having one or more pendant diperoxysuccinyl groups. Also the invention relates to methods of preparing these compounds.

(2) Description of the prior art We know of no reported work on the addition reactions of unsaturated peroxyesters.

Free radical additions to olefins to form carbon-carbon bonds are known. Oragnic reactions, volume XIII, devotes two chapters to such additions. It is know that simple maleate esters and simple fumarate esters will undergo such addition reactions to some extent; however, the fumarates undergo this addition reaction far less readily than do the maleate esters. Thus, Organic Reactions gives 39 examples of maleate ester additions and only 3 examples of fumarate ester additions.

Patrick, J. Org. Chem, 17, 1009 (1952) reports a 76% yield of alpha-butyryl succinic ester from the addition of n-butyraldehyde to diethyl maleate; and a 26% yield of alpha-butyryl succinic ester from the addition of n-butyraldehyde to diethyl fumarate.

Jacobs and Ecke, J. Org. Chem., 28, 3036 (1963) report a 27% yield of addition product of tetrahydrofuran (THF) and diethyl maleate. Maleic anhydride and tetrahydrofuran added at a yield of 61% and 70%. In all these experiments the temperature was held at the reflux temperature of the THF [about 65 0.]. Also, they state the reaction is specific to five membered cyclic ethers.

3,746,735 Patented July 17, 1973 ice We obtained at the Jacobs and Ecke conditions a 39% yield of the addition product of diethyl maleate and tetrahydrofuran and a 14% yield of the addition product of diethyl fumarate and tetrahydrofuran.

SUMMARY OF THE INVENTION We have discovered that diesters of diperoxyfurrnaric acid react with (add to) a great many organic compounds (the more common compounds are simple inert solvents, such as, alcohols and ethers) when the materials are mixed. The reaction is exothermic and the temperature must be controlled to avoid substantial decomposition of the addition product. (Pure di-t-butyl diperoxy fumarate is indefinitely stable at room temperature, about 25 C.).

This addition reaction is completely unexpected be cause the simple fumarate esters are rather inert to free radical addition and even under vigorous conditions give poor yield of the addition product (sometimes called adducts). Even more surprising is the fact that the diesters of diperoxyfumarate add more easily and give almost quantitative yields as compared to maleic anhydride, hitherto considered a very reactive compound in free radical addition reactions.

To illustrate: Maleic anhydride and THF, at reflux temperature, and sunlamp irradiation, gave a 61% yield of product in '6 hours (Jacobs and Ecke). Di-t-butyl diperoxyfumarate and THF, at 0 (zero) C. and sunlamp irradiation, gave a yield of 94% of product in 6 hours.

The process of the invention makes a compound having (including) at least one pair of peroxycarbonyl ester groups in gamma relationship to each other by saturating the double bond of a diester of diperoxyfumaric acid, under controlled conditions of temperature below about +30 C., by means of an organic compound R(X), where (X) is present in excess of the stoichiometric requirement for saturation of said fumaric acid, to obtain a product including at least one diester of a substituted diperoxysuccinic acid, where: (a) each of said ester groups is alkyl, cycloalkyl or aralkyl; and (b) R--(X) is an organic compound having a monovalent atom X readily abstractable by a free radical, R is inert to the peroxycarbonyl groups in said diperoxyfumaric acid diester, and s is equal to at least 1. Desirably the C-X bond of compound R-(X) is characterized by a bond energy of not more than about kcal. per mole.

Particularly suitable R(X) compounds fall in the classes of alcohols, ethers, aldehydes, formate esters, carboxylic acids, mercaptans, orthoesters, acetals, halohydrocarbons, hydrocarbon substituted silanes, and hydrocarbon substituted phosphines.

The compound of the invention has the formula 3 DESCRIPTION OF THE INVENTION AND WORKING EXAMPLES This invention alfords a surprisingly simple process by which a wide variety of relatively complex organic per- 5 oxyesters hitherto unobtainable can be prepared in good to excellent yields. I

The process comprises adding, desirably, a solution of diester of diperoxyfumaric acid in a saturated hydrocarbon, such as pentane, or other inert solvent, to an excess, desirably from a 2 to 1 to 20 to 1 molar ratio of substrate, R(X) to fumarate, preferably about 10 to 1, while vigorous agitation is provided and the reaction temperature is maintained at below about +30, commonly --20 to +30 C., preferably to C.

The reaction may be irradiated with a sun lamp but this is not necessary in most cases. Catalysts such as diisobutyryl peroxide, diisopropyl peroxydicarbonate or acetyl cyclohexanesulfonyl peroxide may be used in place of or in addition to a sun lamp.

The peroxyfumarate (solution) is preferably added slowly over a period of time, for example: over a 4-6 hr. period or even longer. It can be added all at once if the reaction zone temperature is controlled at the desired level.

The reaction mixture is stirred for a time, for example: 1 to 2 hours, after completion of the addition of the peroxyfumarate, then the excess substrate is removed by suitable means, such as vacuum, stripping, fractional distillation or selective extraction. The addition product is usually substantially pure but may be further purified by crystallization or the like methods.

Useful substrate, R--(X) is any compound having a monovalent atom, -X, readily abstractable by a free radical. R is inert to a peroxycarbonyl group under reaction conditions. The most common abstractable atom X, is a hydrogen atom but other atoms, such as chlorine and bromine, can be abstractable. In general, it may be said that any compound, R-(X) where the bond energy of the C-X bond is not more than about 80 kcal. per mole will be an eflective substrate for addition to the double bond of the diperoxyfumarate.

Some illustrations of typical R(X) compounds having a suitable bond energy are given in Table A.

Other factors must be considered such as stabilization of the radical R- by resonance or hyperconjugation and dilfusion of the electron charge over a large atom such as sulfur or phosphorus.

Various classes of compounds R(X), which are use- 4 ful, R--(X), is not limited to these, the invention are:

in the process of (14) molecular arrangements of one or more radicals derived from 1-13, said molecules being characterized by the presence of a plurality of (X) atoms, where:

(a) R is hydrogen, alkyl, cycloalkyl or aralkyl, each having 1-12 carbon atoms;

(b) R -C-R may form a homocyclic group;

(c) R is alkyl, cycloalkyl, aralkyl or aryl;

(d) R; is hydrogen, alkyl, cycloalkyl, aralkyl or aryl;

(e) R -OCR may form a heterocyclic group;

(f) R -C-R may form a homocyclic group;

(g) R O--COR may form a heterocyclic group (I1) R is alkyl, cycloalkyl, aralkyl or halo;

(i) Halo is chloro or bromo;

(j) R is alkyl, cycloalkyl or aralkyl;

(k) R is hydrogen or -C(R --H; and

(m) in (1) not more than one R is hydrogen.

The substrate, R-(X),,, is further illustrated:

(1) Alcohols 'Any primary or secondary alcohol, i.e., not more than one R can be hydrogen, of the defined classes. For example: ethanol, isopropanol, cyclohexanol, and alpha-phenethyl alcohol. Molecular arrangement (12) includes simple diols, triols, etc. having two or more hydroxyl groups, such as hexandiol, glycerol and cyclohexandiol.

(2) Ethers R is alkyl, cycloalkyl, aralkyl or aryl; R is alkyl, cycloalkyl or aralkyl, R OCR may form a heterocyclic system such as tetrahydrofuryl, tetrahydropyranyl;

may form a homocyclic group such as cyclohexyl, cyclopentyl. Illustrations: diisopropyl ether, phenyl isopropyl ether, t-butyl isopropyl ether, diethyl ether, methyl cyclohexyl ether, tetrahydrofuran, Z-methyltetrahydrofuran, poly-ethers such as polyethylene glycols, polypropylene glycols, Carbowaxes and Carbitols, and simple ether glycols such as diethylene glycol.

(3) Aldehydes Illustrations: benzaldehyde, acctaldehyde, formaldehyde, cyclohexanecarboxaldehyde, pivalaldehyde, butyraldehyde, hydrocinnamaldehyde.

' (4) Ketones Illustrations: Acetone, di-n-amyl ketone, methyl ethyl ketone, methyl cyclopropyl ketone, phenyl isopropyl ketone.

(5) Formate esters Illustrations: Methyl formate, benzyl formate, phenyl formate, and cyclopentyl formate.

(6) Carboxylic acids It is preferred that only one R be hydrogen. Any acid coming within this class can be used. Simple polycarboxylic acids come within class (12).

(7) Substituted amides Illustrations: N,N-dimethyl formamide; N,N-dimethylisobutyramide, N,N-diethyl formamide.

(8) Mercaptans Illustrations: Propanethiol, thiophenol, cyclohexanethiol and alpha-mercaptoethylbenzene. Polymercaptans corresponding to glycols, ether glycols, and polyglycols come within class (12).

(9) Orthoesters Illustrations: trimethyl orthoformate, triphenyl orthoformate, tricyclohexyl orthoformate, triisobutyl orthoformate.

(10) Acetals R is alkyl, cycloalkyl, aryl or aralkyl; R is R or hydrogen; (R O) C can be part of a heterocyclic system such as 1,3 dioxolanyl. For example: benzaldehyde-dimethylacetal, 2-phenyl-1,3 dioxolane, butyraldehyde-diethyl acetal.

(11) Halohydrocarbons Halo here means chloro or bromo and includes all those well known members of this class especially the halomethanes, haloethanes, halocyclohexanes, phenyl- (chloro)ethane. The chloro methanes and chloroethanes are preferred; however the halowaxes are especially of interest when a long chain having many pendant diperoxysuccinyl groups is desired.

(12) Hydrocarbon substituted silanes Illustrations: trimethyl silane, tribenzoyl silane, tricyclohexyl silane, tri-t-butylsilane.

(13) Hydrocarbon substituted phosphines Illustrations: Dimethyl phosphine, di-n-propyl phosphine, di-benzyl phosphine, dicyclohexyl phosphine.

(14) Molecular arrangements In addition to the simple polyfunctional molecules mentioned in connection with l-13 above, the invention contemplates as substrates polymers and copolymers containing the above or other functional groups either in the polymer backbone or as pendant groups. Such addition products are useful for the preparation of block and graft polymers and in polymer laminates where the pendant dipersoxy succinyl groups act as bonding sites between the polymer interfaces.

Illustrative polymer substrates include polymers and copolymers of polyvinyl esters, polyacetals, polyethylene glycols, polypropylene glycols, polyvinyl alcohols, polymethacrylic acids and polyesters of diols and dicarboxylic acids.

Substrates containing two or more abstractable hydrogens may be used but can lead to complex mixtures which will be diflicult to purify.

Substrates containing olefinic unsaturations desirably should be avoided since radical reactions will occur at these double bonds to produce byproducts, which may or may not be desirable.

FURTHER ILLUSTRATIVE MATERIAL l Hydroxyl: Isopropanol and DBDPF. Name: t-Butyl gamma-hydroxy-gamma-methyl-beta- (tbutylperoxycarbonyl) peroxyvalerate CH3 H (I) HO (EC7-O O C(CHs):

H3 IO H2 (i-O O C(CHa)a (2) Alkoxy: Tetrahydrofuran and DBDPF. Di-t-butyl alpha-(Z-tetrahydrofuryl) diperoxysuccinate H t H O(3-O O C(CHa):

(3) Beta-carbonyl: n-Butyraldehyde and DBDPF. Di-t-butyl, alpha-butyryldiperoxysuccinate Formula O H2oii-0 O-(t-Bu) (4) Gamma-carbonyl: Methyl isopropyl ketone and DBDPF. t-Butyl 3 (t butylperoxycarbonyl) 4,4 dimethyl-S- oxoperoxyhexanoate (5) Carbalkoxy: Methyl formate and DBDPF. Di t butyl alpha (methoxycarbonyl)diperoxysuccinate o o H H 1; omoo-o- OO-(t-Bu) H2C--(|3I-O O-(t-Bu) (6) Carboxyl: Isobutyric acid and DBDPF.

t-Butyl gamma-carboxy gamma methyl ,B '(t-butylperoxycarbonyl)-peroxyvalerate HtC-C-O O C (CH3):

(7) Amido: N,N-dimethy1 formamide and DBDPF.

7 (8) Thiaalkyl: n-propyl mercaptan and DBDPF. Di-tbutyl alpha-( l-thiabutyl) diperoxysuccinate (9) Orthoester: Trimethylorthoformate and DBDPF. Di-t-butyl alpha-(trimethoxymethyl)diperoxysuccinate ADDITIONAL DEFINITIONS Alkyl: Except where noted otherwise, each alkyl group may include 1 or more carbon atoms. Desirably each has 1-22 carbon atoms. Preferably each has 1-12 carbon atoms.

Cycloalkyl: May be single ring or have two or more fused rings. Desirably the single ring has in the ring 3-12 carbon atoms, and preferably -28 carbon atoms. Preferably the total number of carbon atoms in the radical is 5-12.

Aryl: May be a single benzene ring, or a doubled or higher system, e.g. biphenyl, terphenyl, quaternapthalene, or a fused benzene ring system, e.g. naphthalene, anthracene, phenathrene, or an alkane bridged system, e.g., biphenylmethane, biphenylpropane. Phenyl, biphenyl, naphthalyl and the alkyl substituted radicals are preferred.

Aralkyl: The Ar portion of the radical may be as in Aryl. The alkyl portion has desirably 1-12 carbon atoms and preferably 1-6 carbon atoms.

R(X) R is any organic radical, preferably free of ethylene unsaturation, inert to peroxycarbonyl groups and having valence bonds equal to s. X is a monovalent atom readily abstractable, under these reaction conditions, by a free radical. s may be an integer from 1 to about 500, depending on the type of diperoxysuccinyl compound desired and also the amount of active oxygen to be present in the particular product.

UTILITY As already mentionedf the polymeric products of the invention are useful in graft and block copolymers preparation. All of the products of the invention are useful as free radical initiators in the same maner as other peroxyesters and peroxides, for example, in vinyl polymerization and the curing of unsaturated polyester resins and elastomers.

EXAMPLE OF THE INVENTION AND UTILITY Example 1.The spontaneous decomposition of di-t-butyl diperoxyfumarate in diethyl ether A 250 ml. flask was equipped with a reflux condenser, thermometer and magnetic stirring bar. The flask was surrounded by an ice bath and to the flask was charged 13.0 g. (0.05 mole) of di-t-butyl diperoxyfumarate and 37 g. (0.5 mole) of diethyl ether. When the fumarate ester had dissolved completely, the ice bath was removed and the solution allowed to warm up. The mixture spontaneously warmed up to about 35 and the ether gently refluxed. The mixture was stirred at ambient temperature for sixteen hours.

The ether was removed in vacuo leaving 14.4 g. of a pale yellow viscous oil. The oil was dissolved in a small amount of pentane cooled to 10 and seeded with crystals of di-t-butyl diperoxyfumarate but there was no crystallization (Pentane is the preferred solvent for the recrystallization of di-t-butyl diperoxyfumarate). The pentane was then stripped oif in vacuo and the residue was analyzed for active oxygen (the peroxidic oxygen content). The oil contained 7.00% active oxygen. The active oxygen content of pure di-t-butyl diperoxyfumarate is 12.6%. Therefore it was calculated that 37% of the initial active oxygen content had been lost.

The peroxide oil (11 g.) was redissolved in 200 ml. of diethyl ether and stirred at ambient temperature for 24 hours. The ether was removed in vacuo as before leaving 10 g. of yellow oil. The oil was analyzed and was found not to have lost any further active oxygen.

Thus it is apparent that the peroxidic oil was not impure di-t-butyl diperoxyfumarate since after the initial loss of active oxygen no further loss occurred on prolonged stirring with a fresh quantity of diethyl ether.

Example 2.--The decomposition of di-t-butyl diperoxyfumarate in ethyl alcohol A 0.1 molar solution of di-t-butyl diperoxyfumarate in ethanol was prepared by dissolving the required amount of fumarate ester in ethyl alcohol at -10 C. The solution was kept below 0 C. Ten ml. aliquots of the solution were sealed in tubes and placed in a constant temperature batch at 40. Samples were removed periodically and assayed for active oxygen and for unreacted di-tbutyl diperoxyfumarate by thin layer chromatography. Within one hour of placing the tubes in the bath, all of the di-t-butyl diperoxyfumarate had disappeared even though there was very little loss of active oxygen.

Thus it is evident that some reaction took place between ethanol and di-t-butyl diperoxyfumarate that did not involve the peroxidic oxygen atoms.

Example 3.-The preparation of di-t-butyl alpha-(2-tetrahydrofuryl)diperoxysuccinate A 200 ml., reaction kettle was fabricated having the following specifications: internal diameter 1.5 inches, internal height 7 inches and reactor completely enclosed in a glass jacket for the purpose of circulating a heat exchange liquid usually ice water. The reactor was equipped with a mechanically-operated paddle stirrer, a reflux condenser, thermometer, and an additional funnel. The reactor was irradiated by a Westinghouse 275 watt sun lamp situated about 10 inches from the outer wall of the reactor.

The reactor was charged with ml. of tetrahydrofuran freshly distilled from lithium aluminum hydride. A saturated solution of 39 g. (0.15 mole) of di-t-butyl diperoxyfumarate in pentane was placed in the addition funnel. The funnel was covered with aluminum foil to prevent irradiation of the diperoxyfumarate solution. The air in the reactor was displaced by nitrogen. The sun lamp was turned on and dropwise addition of the fumarate solution was begun. The addition required five hours and there was an additional 30 minutes of stirring after addition was complete. The reaction temperature was maintained at 12 C. by circulating ice water through the reactor jacket.

The reaction mixture was then stripped on a rotating vacuum evaporator at 25 and 0.1 mm. pressure until there was no further weight loss.

The residual oil weighed 46.7 g. (94% of theory) and contained 8.94% active oxygen. The theoretical active oxygen for di-t-butyl alpha-(2-tetrahydrofuryl)diperoxysuccinate is 9.64%. The assay based on active oxygen was therefore 92.8%.

A duplicate run made under identical conditions gave 47.2 g. (94.8% of theory) and an active oxygen content of 8.83%. (91.6% of theory).

In order to establish the structure of the product, a 10 gram sample was dissolved in 50 ml. of absolute alcohol and subject to hydrogenolysis at 50 p.s.i.g. and 25 C. using a 1% platinum on charcoal catalyst in a Parr Hydrogenation Apparatus. Peroxyesters are readily reduced to the parent acid and the alcohol from which the peroxy portion of the ester was derived.

II II RC-OOR H. noon ROH After no further hydrogen was absorbed, the ethanolic solution was filtered to remove the catalyst and the filtrate was stripped in vacuo on a rotating evaporator, leaving a solid residue weighing 4.2 g. The solid was triturated with benzene, filtered and dried twelve hours in a vacuum oven at 50 C. The solid melted at 12833 C. on a Fisher-Johns melting point block. The neutralization equivalent was found to be 99.8. The theoretical value for alpha-(2-tetrahydrofuryl)succinic acid is 94.1.

Since this acid has not been disclosed in the literature, an authentic sample was prepared by the saponification of diethyl alpha-(Z-tetrahydrofuryl)succinate which was prepared by the addition of tetrahydrofuran to diethyl maleate. The authentic acid after being recrystallized twice from a chloroform-cyclohexane solution melted at l28130. The free acid has a tendency to absorb moisture from the air. A carefully dried sample had a neutralization equivalent of 94.1 (theory 94.2). The infra-red spectra of mineral oils mulls of the authentic acid and the acid obtained by hydrogenolysis of the perester were identical.

Example 4.The preparation of di-t-butyl alpha-acetyld-iperoxysuccinate Into the reactor described in Example 3 was charged 88 g. (20 moles) of acetaldehyde. The reactor was irradiated by the sun lamp. A saturated solution of 39.0 g. (0.15 mole) of di-t-butyldiperoxyfumarate in pentane was added over a 7 hour period to the stirred acetaldehyde while the reaction temperature was kept at 0. After the addition was complete, the reaction mixture was stirred for 30 minutes.

The reaction mixture was stripped in vacuo of excess acetaldehyde on a rotating evaporator. The residue which weighed 66 g. was dissolved in 200 ml. of diethyl ether and was extracted six times with 100 ml. portions of water. The water washings were discarded and the ethereal solution was dried over magnesium sulfate. The drying agent was removed by filtration and the filtrate was stripped in vacuo on a rotating evaporator. The residue was a pale yellow oil, weighed 41.9 g. (92% of theory), and assayed 74.8% based on active oxygen.

A drop of the yellow oil when added to a dilute aqueous ferric chloride solution showed the deep red color characteristic of beta-ketoesters. Neither acetaldehyde nor di-t-butyl diperoxyfumarate give this color.

A 10 g. portion of peroxide was subject to hydrogenolysis as described in Example 3. A platinum oxide catalyst was used instead of platinum on charcoal when it was observed that addition of the platinum catalyst caused violent decomposition of the peroxide. This characteristic property was observed with all alpha-acyl-diperoxy-succinates that were prepared. Neither di-t-butyl diperoxyfumarate nor the adducts derived from substrates other than aldehydes were decomposed by platinum on charcoal.

Filtration and evaporation of the hydrogenolysis mixture left an oily liquid acid having the properties of levulinic acid. The expected hydrogenolysis product alphaacetylsuccinic acid is unstable and rapidly loses carbon dioxide to give levulinic acid. Beta-keto-carboxylic acids are prone to decarboxylation.

II II II CHaCCHC-OH CHQCCHQ Example 5.The preparation of di-t-butyl alpha-butyryldiperoxysuccinate 10 39.0 g. (0.15 mole) di-t-butyl diperoxyfumarate was added over a 5.5 hour period to the butyraldehyde maintained at 0 C. Stirring was continued for two hours after completion of the addition.

The reaction mixture was stripped at room temperature on a rotating evaporatof at an ultimate vacuum of 0.1 mm. The colorless residue weighed 51.9 g. (104% of theory) and assayed 87.2% based on active oxygen.

A 5 gram sample was hydrogenolyzed using a platinum oxide catalyst as described in Examples 3 and 4. After removal of the catalyst and solvent, there remained a lowmelting colorless solid. Recrystallization from cycohexane afforded 1 g. of shiny crystals melting at 47 and having a neutralization equivalent of 146.1. The theoretical n utralization equivalent of 4-oxoheptanoic acid is 144.2 and the reported melting point is 49-50, Wiley and Herrell, J. Org. Chem. 25, 903 (1960). alpha-Butyrylsuccinic acid spontaneously decarboxylates to 4-oxoheptanoic acid.

A 30 g. sample of the crude di-t-butyl 'alphabutyryldiperoxysuccinate solidified on standing two weeks in a refrigerator. The solid was recrystallized from pentane at 0 C. The colorless crystalline product melts at 30 C. and assayed 96.0% based on active oxygen.

Example 6.-The addition of diisopropyl ether to di-tbutyl-diperoxy fumarate The reactor described in Example 3 was charged with 102 g. (1.0 mole) of diisopropyl ether and was illuminated by a sun lamp. The ether was vigorously stirred under a nitrogen atmosphere while a pentane solution containing 26.0 g. (0.1 mole) of di-t-butyl diperoxyfumarate was added over a period of 6.5 hours. The reaction mixture was stirred for an additional hour. The temperature was kept at 0 to 2 during the reaction.

The excess diisopropyl ether and pentane were removed in vacuo on a rotating evaporator. The liquid residue weighed 31.0 g. (86% of theory) and assayed 83.9% based on active oxygen.

Hydrogenolysis over a platinum on charcoal catalyst of 12 g. of the adduct gave a very hygroscopic solid dicarboxylic acid having a neutralization equivalent of 110.3. The acid was identified as 3-carboxy-4-methyl-4-isopropoxyvaleric acid (I) having a theoretical neutralization equivalent of 109.12.

The new peroxide therefore is t-butyl 3-(t-butylperoxycarbonyl)-4-methyl 4 isopropoxyperoxyvalerate (I-I) arising from the addition of a molecule of diisopropyl other across the double 'bond of di-t-butyl diperoxyfumarate.

Example 7.The addition of polyethylene glycol to di-tbutyl diperoxyfumarate Into the reactor described in Example 3 was charged g. of Polyglycol E600, a product of the Dow Chemical Corporation consisting of a polyethylene glycol having a number average molecular weight of 600. The air in the reactor was displaced with nitrogen. The reactor was irradiated by a sun lamp while a pentane solution of 43.3 g. (0.167 mole) of di-t-butyl diperoxyfumarate was added over a 5.5 hour period. The reaction mixture was maintained at 25 C., the lowest temperature at which the mixture remained liquid. After a total reaction time of 7 hours, the mixture was transferred to an open top reactor and extracted twice with 100 ml. portions of pentane in order to remove any unreacted peroxyfumarate ester. The second extract contained no measurable active oxygen.

HOOHgCH1(OCHIOH2)nOH0112(0 GHgCH2) O CHgCHgOH H -CH:

=0 (CHmC 0( ()0 0 (CH1):

Example 8.The addition of isopropyl alcohol to di-t-butyl diperoxyfumarate A pentane solution of 39.0 g. (0.15 mole) of di-t-butyl diperoxyfumarate was added over a 6.5 hour period to 120 g. (2.0 mole) of isopropyl alcohol contained in the reactor described in Example 3. The reactor was illuminated by a sun lamp and kept at 0 during the addition and for a further 90 minutes of stirring.

A solid product began to separate from the reaction mixture toward the end of the reaction. The reaction mixture was concentrated in vacuo to one-half its volume and then kept at 0 for two hours during which a colorless solid crystallized. The product was separated by filtration, the filter cake washed with a little cold isopropyl alcohol and dried by passing air through the filter cake. The solid melted at 6570 and weighed 12 g. Additional product was isolated by concentrating the mother liquors.

The isopropyl alcohol mother liquors contained t-butyl hydroperoxide indicating that some transesterification had occurred during the reaction as shown in equation.

CH: Ho( :0H( i000(oHa) CH; O (CHaMCHOH HgC-C-0OC(CHz)z CH; O HO('JCH-(%OOC(OH:):

Hz 0 OH; or (CHr)aCOOH Hie-00C (IV) CH1 CH3 0 CH1 HO('J-CH ooh CH: 0 CH! Hg (I!-OOC(GH3) The solid product assayed 80.7% based on active oxygen analysis. Recrystallization of the product from benzene-cyclohexane failed to improve the assay indicating that byproducts IV and/or V co-crystallized along with III.

In order to establish that the structure of the product was III, 6 g. of the solid product was treated with hydrogen and a platinum catalyst as described in previous examples. The hydrogenolysis product was recrystallized from ethanol, melted at 174-476 and was identified as beta carboxy gamma methyl gamma valerolactone formed by spontaneous lactonization of the diacid as shown in equation.

The neutralization equivalent for VI was found to be 162 (theoretical value is 15 8). A portion of VI was carefully saponified with warm aqueous sodium hydroxide and the excess base was back-titrated with 0.1 N acid using a pH meter to determine the end point. The saponification equivalent (after correction for the free carboxylic acid) was found to be 168 (theory for VI is 158).

Example 9.The preparation of di-t-butyl alpha-pivaloyldiperoxysuccinate The title compound was prepared by adding a pentane solution of 39 g. (0.15 mole) of di-t-butyl diperoxyfumarate to 100 g. (1.16 mole) of pivalaldehyde (trimethylacetaldehyde) under conditions equivalent to those described in Example 5. From the vacuum-stripped crude reaction mixture was isolated 16.9 g. of crystalline di-tbutyl alpha-pivaloyldiperoxysuccinate (VII) melting at 65 and assaying 103% based on the active oxygen content. Additional product of slightly lower assay was isolated from the mother liquors.

(VII) Example 10.The preparation of di-t-butyl alpha- (methoxycarbonyl) diperoxysuccinate A pentane solution of 39.0 g. (0.15 mole) of di-t-butyl diperoxyfumarate was added over a six hour period to ml. of methyl formate contained in the reactor described in Example 3. The reactor was illuminated by a sun lamp and kept at 0-5" C. during the addition and for a further 90 minutes of stirring.

The reaction mixture was stripped on a rotating evaporator to an ultimate vacuum of 3 mm. in order to remove the pentane and unreacted methyl formate. The residue weighed 38.8 g. (81% of theory) and assayed 100% based on active oxygen determination.

An 8 g. sample was hydrogenolyzed using a platinum on charcoal catalyst. Work-up of the reaction mixture yielded an oily solid which was purified by precipitating it from acetone by the addition of pentane. The neutralization equivalent of the solid was 69 (theory for VIII is 88; theory for IX is 54). Therefore, the hydrogenolysis product is probably a mixture of VIII and IX.

o Hm-d-OH mo-ii-orr (VIII) (IX) One g. of the hydrogenolysis product was heated on a steam bath for 1 hour with 15 ml. of water containing 2 drops of concentrated hydrochloric acid until the mixture was completely homogeneous. The yellow solution was Example 13.The addition of trimethyl orthoformate to evaporated to dryness leaving a semicrystalline solid. This di-t-butyl diperoxyfumarate solid was dissolved in ethyl acetate and reprecipitated by A pentane solution of 39 g. (0.15 mole) of d1-t-butyl the g g g g iffi fii g diperoxyfumarate was added over a 5.5 hour period to a i gw y zg g a e 3 2 5 5 106 g. (1.0 mole) of trimethyl orthoformate contained me 6 S01 me 6 W1 ecomposl Ion a in the reactor described in Example 3. The reactor was The melting point reported for 1,1,2-ethanetricarboxylic o o w 2 e Elia-satin;strai s. The Peroxldlc pr9duct is therefore dlt'butyl alpha The reaction mixture was stripped at an ultimate vacu- (methoxycarbonyl) dlperoxysuccmate 10 um of 1 mm. using a rotating evaporator leaving a viscous yellow oil weighing 36.3 g. (66% of theory) and assaying 84.2% based on active oxygen content. The structure of 011.0 i z- -ii-ooowm the product is shown below (XIII).

OCH: 0 1 I H,oooo om)t CHaO ocn 0OO(OH3)| (X) 0 CH3 mo-d-ooowm).

Example 14.Preparation of a polyethylene glycolpolystyrene graft copolymer Example 11.-The addition of methyl isopropyl ketone to di-t-butyl diperoxyfumarate A pentane solution of 39.0 g. (0.15 mole) of di-t- The polyethylene glycol-di-t-butyl diperoxy fumarate butyl diperoxyfumarate was added over a 4 hour period adduct described in Example 7 was used to initiate to 129 g. (1.5 moles) of methyl isopropyl ketone constyrene polymerization at 100 C.

tained in the reactor described in Example 3. The reactor At an initiator concentration of 5 10 active oxygen was illuminated by a sun lamp and kept at 0 C. during equivalents per deciliter of styrene the rate of initiation the addition and for a further 3 hours of stirring. was 966x10 mole/liter/min. as determined by The reaction mixture was then stripped at an ultimate dilatometry. vacuum of 0.1 mm. on a rotating evaporator leaving 45.2 The resultant polymer was a mixture of polystyrene g. (86.5% of theory) of a pale yellow liquid containing homopolymer and a polyethylene glycol-polystyrene graft 9.11% active oxygen (theory for (X1) 9.24%). Assay copolymer with the probable structure (XIV) shown bewas therefore 98.7%. low where m+n=10 to 16, x and y are from 10 to 500.

Hgk CsHs CsHs CsHs 30115 1 (XIV) 0 CH3 0 The polystyrene homopolymer was removed by extraction with be ne 'n wh' th 1 I g soluble. nze 1 10h e graft copo ymer 1s in H3 E Example 15 OH OOG CH 2 In order to demonstrate the capability of this process (XI) to tailor-made peroxides of a desired decomposition rate, the half-lives of several of the peroxides, described in the preceding examples, were determined. Dilute benzene solutions, usually 0.1 molar, of the peroxides were pre- A pentane solution of 39.0 g. (0.15 mole) of di-t-butyl pared, aliquots were sealed into glass tubes and the glass diperoxyfumarate was added over a 7 hour period to 132 tubes were immersed in constant temperature baths. Samg. (1.5 moles) of isobutyric acid contained in the reactor ples were periodically withdrawn and were assayed for described in Example 3. The reactor was illuminated by active oxygen content by standard analytical methods. a sun lamp and kept at 0 C. during the addition and for 5 All the peroxides tested followed first order decomposi- Example 12.The addition of isobutyric acid to di-t-butyl diperoxyfumarate a further 15 minutes of stirring. tion kinetics. The half-lives are listed in Table 15.

The reaction m xture was st1rred into 800 ml. of ice TABLE 15 SELECTED HALFJIVES OF PEROXIDES 'water. The organic layer was separated and washed 4 times with 500 ml. portions of water. The organic layer $33: was diluted with an equal volume of ether and dried over turn t1}: sodium sulfate. The solution, filtered free of drying agent, Sample Q) (11) was stripped in vacuo on a rotating evaporator to a A Di-t-butyldiperoxyfumarate 85 5.5 weight of 64 g. Since the theoretical yield was 52.3 g., there was still unreacted isobutyric acid in the product. B--.-. Dilg-butylalpha-(i-tetrahydrofuryl) 85 30.1 The water extraction procedure was repeated and the 65 Pemxysuccma C Di-t-but lal h -but ldi ero s inat 51.7 product after drylng and stripping weighed 37.7 g. (72% do 9.6

6 i, of theory) and assayed 803% based on actlve oxygen D Dl-t-butyl alpha-pivaloyldiperoxysuccinate. 85 19.0 content. The structure of the product 1s shown below E Di-lz-bultylldiiperoxyfumaratepolyethylene 100 5.5

gyco a 11 (XII) F t-Butyl 3-(t-butylperoxycarbonyl)-4-methy1- 85 26.6

0 CH3 0 70 4-1sopropoxyperoxyvalerate. Hog-4 3 {5 OOC(CH) a 8 Example .16 CH3 0 Rates of polymerization of styrene were determined by dilatometry using the peroxides listed in Table 15 as (XII) initiators. The concentation of initiator was 5 X 10- active v was found to contain 0.11% active oxygen. One of the oxygen equivalent per deciliter of styrene. The results are (CHQQCOO 000mm),

listed in Table 16.

TABLE m-rnnoxrnn-rmrmrnn POLYMERIZATION OF STYRENE H C-CH-(CH CH)w-CH -O-(OH;CH),'CH,CH 0JJOH:

Rate of as. ii" if 22 Z? 1...... an: senate; 10 (XVI; Sample 4 $12 Example l9.dAdd-ition r N,N-dimethylformamide to 100 55x10 i-t-butyl dlperoxyfumarate 32 Z; A pentane solution of the diperoxyfumarate was added over a five hour period to N,N-dimethyl formamide, the 15 reaction zone was maintained at 0 C. The reaction porduct mixture was diluted with water and the addition product extracted with benzene; the extract was dried over magnesium sulfate and stripped in 'vacuo. The prod- A slurry of 17 parts by a weight of Gantrez resi not was an amber oil which is very unstable at room (a copolymer of methyl vinyl ether and maleic anhydride, temperature- The Produot has the structure: a product of the General Aniline and Film Corporation),

Example 17.--The heterogeneous addition reaction of a polyvinyl ether and di-t-butyl diperoxyfumarate 17 parts di-t-butyl diperoxyfumarate and 66 parts of ii-oo-(t-Bu) benzene was stirred for 7 hours at 23 While being irradiated with a sun lamp. 25 O 1 The slurry was filtered and the solids were washed well HaCNC-CH with benzene to remove any unreacted di-t-butyl CH3 diperoxyfumarate. The solid polymeric product was found to contain 0.09% active oxygen corresponding to an adduct containing 1.9 g. of di-t-butyl diperoxy fumarate and 98.1% g. of Gantrez resin. A control run in (XVII) Thus having described the invention, what is claimed which no diperoxyfumarate was added contained no deis. tectable active oxygen. 1. A process for preparing a substituted diperoxy-suc- In another run, a slurry of 88.2 parts hexane, 9.8 parts cinic acid diester of the formula Gantrez resin and 2.0 parts of di-t-butyl diperoxyfumarate was used, a polymeric product was isolated con- I H taining0.1l% active oxygen. Rl-00'( JC- -00-R.

We believe the product to be formed by a free radical l RPJFRI addition involving the carbon-hydrogen bonds adjacent to the ether oxygens in the resin to give structure XV shown 40 H below' which process comprises saturating the double bond of Example 18.-The homogeneous addition reaction of a polyvinyl ether or polyvinyl acetate and di-t-butyl diat a temperature of from about -20 C. to about +30 peroxyfumarate C. by means of the addition of an organic alcohol, (a) A solution of 92 parts of acetone, 6.6 parts of 1 Gantrez resin and 1.4 parts of di-t-butyl diperoxy- 5 0- fumarate was stirred for 5 hours at 23 while being irradiated with a sun lamp.

The product was precipitated by pouring the acetone solution into an excess of hexane. The precipitated polymer was separated by filtration. The polymer was purified by dissolving it in acetone and reprecipitating it from hexane. After two precipitations, the polymer was analyzed for active oxygen. The polymer contained 0.16% active oxygen. The polymer from a control run contained no detectable active oxygen.

. (b) A similar reaction was carried out with polyvinyl acetate instead of Gantrez resin. The resultant polymer having a readily extractable hydrogen atom, where:

R; is hydrogen, alkyl of 1-12 carbons, cycloalkyl of 3-12 carbons of hydrocarbon aralkyl of 7-12 carbons, not more than one R being hydrogen, and R CR can form a homocyclic group; and R is tertiary alkyl, tertiary cycloalkyl or hydrocarbon tertiary aralkyl of 4-12 carbons. 7 2. Claim 1 wherein the reaction mixture is subjected to ultraviolet radiation.

3. Claim 1 wherein R is tertiary butyl. 4. Claim 3 wherein structures (XVI) of the polymeric product is shown be- 7 v 5. Claim 3 wherein both R s are methyl. 9. Claim 7 where both Rfs are methyl.

6. A compound of the formula V o H 0 References Cited g g g UNITED STATES PATENTS 5 2,698,863 1/1955 Dickey 260-453 R H 3,576,826 4/1971 Baiford et al. 260-453 R where: OTHER REFERENCES 1 is y gen, or alkyl of 1-12 carbons, not more Walling et al.: Free Radical Addis. to Olefins, etc., than one R being hydrogen, a 1 1 can 10 1963, Org. Reactions, vol. 13 pp. 91, 116, 117, 135 and form a homocycl1c group; and 136, Wiley & Sons, New York, NY. (1963). R 1s tertiary alkyl of 4-12 carbons. 7. Claim 6 where R; is tertiary butyl. LEWIS GOTTS, Primary Examiner Clalm 7 Where 15 G. HOLLRAH, Assistant Examiner 

